Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057522831

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057522831(A;A)
Make rs1057522831(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position178551261
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs1057522831
dbSNP (classic)rs1057522831
ClinGenrs1057522831
ebirs1057522831
HLIrs1057522831
Exacrs1057522831
Gnomadrs1057522831
Varsomers1057522831
LitVarrs1057522831
Maprs1057522831
PheGenIrs1057522831
Biobankrs1057522831
1000 genomesrs1057522831
hgdprs1057522831
ensemblrs1057522831
geneviewrs1057522831
scholarrs1057522831
googlers1057522831
pharmgkbrs1057522831
gwascentralrs1057522831
openSNPrs1057522831
23andMers1057522831
SNPshotrs1057522831
SNPdbers1057522831
MSV3drs1057522831
GWAS Ctlgrs1057522831
Max Magnitude0
ClinVar
Risk rs1057522831(A;A)
Alt rs1057522831(A;A)
Reference Rs1057522831(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179415988C>T
CLNSRC
CLNACC RCV000441617.1,